Novel autosomal dominant TNNT1 mutation causing nemaline myopathy.

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Advances in pediatrics in 2017: current practices and challenges in allergy, endocrinology, gastroenterology, genetics, immunology, infectious diseases, neonatology, nephrology, neurology, pulmonology from the perspective of Italian Journal of Pediat

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Novel autosomal dominant TNNT1 mutation causing nemaline myopathy.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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Novel autosomal dominant TNNT1 mutation causing nemaline myopathy.

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Novel autosomal dominant TNNT1 mutation causing nemaline myopathy.

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Novel autosomal dominant TNNT1 mutation causing nemaline myopathy.

@en

Novel autosomal dominant TNNT1 mutation causing nemaline myopathy.

@nl

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Novel autosomal dominant TNNT1 mutation causing nemaline myopathy.

@en

Novel autosomal dominant TNNT1 mutation causing nemaline myopathy.

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P1476

Novel autosomal dominant TNNT1 mutation causing nemaline myopathy.

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Clotilde Lagier-Tourenne

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Fernande Freyermuth

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Michael W Lawlor

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Shailendra B Patel

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Thomas L Winder

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Molecular basis of cardiac performance. Plasticity of the myocardium generated through protein isoform switches

Mutations in the nebulin gene associated with autosomal recessive nemaline myopathy

A method and server for predicting damaging missense mutations

Protein Structure-Function Relationship at Work: Learning from Myopathy Mutations of the Slow Skeletal Muscle Isoform of Troponin T

NEMALINE MYOPATHY. A NEW CONGENITAL MYOPATHY

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scholarly article

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10.1002/MGG3.325

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Chamindra G Konersman

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2017-08-21T00:00:00Z

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29178646

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5702563

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Novel autosomal dominant TNNT1 mutation causing nemaline myopathy.

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P2860

P2860

Novel autosomal dominant TNNT1 mutation causing nemaline myopathy.

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P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P698

P932